Variant report

Variant	nsv1034223
Chromosome Location	chr6:4030708-4060347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:531)
CpG islands
(count:122)
Chromatin interactive
region (count:37)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:4055679-4056030	K562	blood:	n/a	n/a
2	ARID3A	chr6:4059355-4059765	K562	blood:	n/a	n/a
3	ARID3A	chr6:4055694-4056061	HepG2	liver:	n/a	n/a
4	BACH1	chr6:4036412-4036423	K562	blood:	n/a	n/a
5	BHLHE40	chr6:4055726-4055996	K562	blood:	n/a	n/a
6	CCNT2	chr6:4055675-4055905	K562	blood:	n/a	n/a
7	CEBPB	chr6:4036437-4036606	HepG2	liver:	n/a	n/a
8	CEBPB	chr6:4037090-4037287	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:4055713-4055854	A549	lung:	n/a	n/a
10	CTCF	chr6:4032760-4032910	HMF	breast:	n/a	n/a
11	CTCF	chr6:4059490-4059566	K562	blood:	n/a	n/a
12	CTCF	chr6:4059500-4059650	HRE	kidney:	n/a	n/a
13	CTCF	chr6:4059420-4059570	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr6:4059516-4059575	NHEK	skin:	n/a	n/a
15	CTCF	chr6:4055800-4055950	HCT-116	colon:	n/a	chr6:4055887-4055908
16	CTCF	chr6:4059420-4059570	HAc	cerebellar:	n/a	n/a
17	CTCF	chr6:4055803-4055936	GM10248	blood:	n/a	chr6:4055887-4055908
18	CTCF	chr6:4055783-4055952	SK-N-SH_RA	brain:	n/a	chr6:4055887-4055908
19	CTCF	chr6:4055820-4055970	HBMEC	blood vessel:	n/a	chr6:4055887-4055908
20	CTCF	chr6:4055839-4055911	GM20000	blood:	n/a	chr6:4055887-4055908
21	CTCF	chr6:4055618-4056162	HCT-116	colon:	n/a	chr6:4055887-4055908
22	CTCF	chr6:4055848-4055932	GM12878	blood:	n/a	chr6:4055887-4055908
23	CTCF	chr6:4059460-4059610	WI-38	lung:	n/a	n/a
24	CTCF	chr6:4055820-4055970	NHDF-neo	bronchial:	n/a	chr6:4055887-4055908
25	CTCF	chr6:4055816-4055962	Spleen_OC	spleen:	n/a	chr6:4055887-4055908
26	CTCF	chr6:4055780-4055930	HUVEC	blood vessel:	n/a	chr6:4055887-4055908
27	CTCF	chr6:4055760-4055910	GM12865	blood:	n/a	chr6:4055887-4055908
28	CTCF	chr6:4055732-4055991	A549	lung:	n/a	chr6:4055887-4055908
29	CTCF	chr6:4055840-4055990	Hela-S3	cervix:	n/a	chr6:4055887-4055908
30	CTCF	chr6:4055800-4055950	HMEC	breast:	n/a	chr6:4055887-4055908
31	CTCF	chr6:4059332-4059700	IMR90	lung:	n/a	n/a
32	CTCF	chr6:4059460-4059610	AG09319	gingival:	n/a	n/a
33	CTCF	chr6:4055780-4055930	AG10803	skin:	n/a	chr6:4055887-4055908
34	CTCF	chr6:4055800-4055950	A549	lung:	n/a	chr6:4055887-4055908
35	CTCF	chr6:4055759-4055972	MCF-7	breast:	n/a	chr6:4055887-4055908
36	CTCF	chr6:4055780-4055930	HFF-Myc	foreskin:	n/a	chr6:4055887-4055908
37	CTCF	chr6:4059440-4059590	NB4	blood:	n/a	n/a
38	CTCF	chr6:4059440-4059590	HCFaa	heart:	n/a	n/a
39	CTCF	chr6:4055802-4055942	GM10266	blood:	n/a	chr6:4055887-4055908
40	CTCF	chr6:4059460-4059610	HMEC	breast:	n/a	n/a
41	CTCF	chr6:4055800-4055950	HEEpiC	esophagus:	n/a	chr6:4055887-4055908
42	CTCF	chr6:4055780-4055930	MCF-7	breast:	n/a	chr6:4055887-4055908
43	CTCF	chr6:4059360-4059510	GM12875	blood:	n/a	n/a
44	CTCF	chr6:4055760-4055910	AoAF	blood vessel:	n/a	chr6:4055887-4055908
45	CTCF	chr6:4055800-4055950	HRE	kidney:	n/a	chr6:4055887-4055908
46	CTCF	chr6:4055654-4055984	K562	blood:	n/a	chr6:4055887-4055908
47	CTCF	chr6:4059420-4059570	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr6:4059440-4059590	HPF	lung:	n/a	n/a
49	CTCF	chr6:4059420-4059570	HPF	lung:	n/a	n/a
50	CTCF	chr6:4055840-4055990	HCT-116	colon:	n/a	chr6:4055887-4055908

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:4056654-4056704	GM12878	blood:	n/a
2	chr6:4032322-4032372	SKMC	muscle:	n/a
3	chr6:4032322-4032372	HUVEC	blood vessel:	n/a
4	chr6:4032322-4032372	HCF	heart:	n/a
5	chr6:4056654-4056704	Hepatocyte	liver:	n/a
6	chr6:4032322-4032372	HCM	heart:	n/a
7	chr6:4032322-4032372	BE2_C	brain:	n/a
8	chr6:4032322-4032372	SK-N-MC	brain:	n/a
9	chr6:4032322-4032372	GM12878	blood:	n/a
10	chr6:4032322-4032372	U87	brain:	n/a
11	chr6:4032322-4032372	HRPEpiC	eye:	n/a
12	chr6:4056654-4056704	Caco-2	colon:	n/a
13	chr6:4056654-4056704	Hela-S3	cervix:	n/a
14	chr6:4056654-4056704	BE2_C	brain:	n/a
15	chr6:4056654-4056704	U87	brain:	n/a
16	chr6:4032322-4032372	HMEC	breast:	n/a
17	chr6:4056654-4056704	HEK293	kidney:	embryo
18	chr6:4056654-4056704	SKMC	muscle:	n/a
19	chr6:4032322-4032372	NHBE	bronchial:	n/a
20	chr6:4032322-4032372	Hepatocyte	liver:	n/a
21	chr6:4056654-4056704	A549	lung:	n/a
22	chr6:4032322-4032372	CMK	blood:	n/a
23	chr6:4056654-4056704	NB4	blood:	n/a
24	chr6:4032322-4032372	NB4	blood:	n/a
25	chr6:4056654-4056704	HAEpiC	amniotic membrane:	n/a
26	chr6:4056654-4056704	AG04450	lung:	fetal
27	chr6:4032322-4032372	PANC-1	pancreas:	n/a
28	chr6:4056654-4056704	GM19239	blood:	n/a
29	chr6:4032322-4032372	HRCEpiC	kidney:	n/a
30	chr6:4032322-4032372	HEK293	kidney:	embryo
31	chr6:4056654-4056704	PANC-1	pancreas:	n/a
32	chr6:4056654-4056704	SK-N-MC	brain:	n/a
33	chr6:4056654-4056704	AG09319	gingival:	n/a
34	chr6:4056654-4056704	HCT-116	colon:	n/a
35	chr6:4032322-4032372	H1-hESC	embryonic stem cell:	embryo
36	chr6:4032322-4032372	NH-A	brain:	n/a
37	chr6:4032322-4032372	NT2-D1	testis:	n/a
38	chr6:4032322-4032372	HEEpiC	esophagus:	n/a
39	chr6:4056654-4056704	HEEpiC	esophagus:	n/a
40	chr6:4032322-4032372	HepG2	liver:	n/a
41	chr6:4056654-4056704	ovcar-3	ovarian:	n/a
42	chr6:4056654-4056704	MCF-7	breast:	n/a
43	chr6:4032322-4032372	SK-N-SH	brain:	n/a
44	chr6:4032322-4032372	NHDF-neo	bronchial:	n/a
45	chr6:4056654-4056704	BJ	skin:	n/a
46	chr6:4032322-4032372	PrEC	prostate:	n/a
47	chr6:4056654-4056704	GM06990	blood:	n/a
48	chr6:4032322-4032372	IMR90	lung:	fetal
49	chr6:4056654-4056704	HCPEpiC	choroid plexus:	n/a
50	chr6:4056654-4056704	HUVEC	blood vessel:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:4040955..4045707-chr6:4056854..4061183,4	K562	blood:
2	chr6:4040955..4043384-chr6:4055982..4058354,2	K562	blood:
3	chr6:4019656..4024130-chr6:4049502..4053557,5	K562	blood:
4	chr6:4032673..4035908-chr6:4133306..4136928,3	K562	blood:
5	chr6:4047640..4049812-chr6:4050419..4052477,2	K562	blood:
6	chr6:4038263..4039862-chr6:4134897..4137709,2	K562	blood:
7	chr6:4041672..4043824-chr6:4045447..4047327,2	K562	blood:
8	chr6:4020118..4022120-chr6:4056131..4059470,3	K562	blood:
9	chr6:4060216..4062981-chr6:4075030..4077501,2	K562	blood:
10	chr6:4038778..4041215-chr6:4053376..4056511,3	K562	blood:
11	chr6:4054760..4058464-chr6:4059155..4063115,3	K562	blood:
12	chr6:4040955..4043384-chr6:4055982..4058354,2	K562	blood:
13	chr6:4020118..4023028-chr6:4056131..4059224,3	K562	blood:
14	chr6:4040702..4042424-chr6:4053690..4055352,2	MCF-7	breast:
15	chr6:4055445..4056340-chr6:4155713..4156846,7	MCF-7	breast:
16	chr6:4028831..4031287-chr6:4036762..4038372,2	MCF-7	breast:
17	chr6:4016440..4019187-chr6:4054276..4058013,4	K562	blood:
18	chr6:4050759..4052710-chr6:4054373..4057120,2	K562	blood:
19	chr20:2451288..2451992-chr6:4047392..4048214,2	NB4	blood:
20	chr6:4047787..4048628-chr7:33396481..33397227,2	MCF-7	breast:
21	chr6:4040955..4045707-chr6:4056854..4061183,4	K562	blood:
22	chr6:4054760..4058464-chr6:4059155..4063115,3	K562	blood:
23	chr6:4041672..4043824-chr6:4045447..4047327,2	K562	blood:
24	chr6:4056059..4057941-chr6:4133460..4135296,2	K562	blood:
25	chr6:4055416..4056150-chr6:4210745..4211284,2	MCF-7	breast:
26	chr6:4050182..4052432-chr6:4060847..4064150,3	K562	blood:
27	chr6:4057382..4058933-chr6:4121513..4123123,2	K562	blood:
28	chr3:79751071..79751988-chr6:4044472..4045061,2	MCF-7	breast:
29	chr6:4019901..4021767-chr6:4032581..4035292,2	MCF-7	breast:
30	chr6:4038415..4040524-chr6:4062857..4065779,3	K562	blood:
31	chr6:4021573..4023167-chr6:4032641..4035084,2	MCF-7	breast:
32	chr6:4034929..4037283-chr6:4138355..4141166,2	K562	blood:
33	chr6:4021626..4023220-chr6:4042242..4044660,2	MCF-7	breast:
34	chr6:4049071..4052432-chr6:4060927..4063181,3	K562	blood:
35	chr6:4046276..4049820-chr6:4052310..4055937,3	K562	blood:
36	chr6:4046276..4049820-chr6:4052310..4055937,3	K562	blood:
37	chr6:4039390..4041631-chr6:4045739..4048422,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf146-4	chr6:4050663-4050752	NONHSAT107278
2	lnc-C6orf146-4	chr6:4050695-4050785	NONHSAT147378
3	lnc-C6orf146-4	chr6:4049668-4049849	NONHSAT107278

No data

(count:1 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PRPF4B	hsa-miR-30a-5p	chr6:4047429-4047449

Variant related genes	Relation type
FAM217A	TF binding region
PRPF4B	TF binding region
FAM217A	CpG island
PRPF4B	CpG island
ENSG00000252668	chromatin interactions
ENSG00000254821	chromatin interactions
ENSG00000272248	chromatin interactions
ENSG00000230648	chromatin interactions
ENSG00000198721	chromatin interactions
ENSG00000125835	chromatin interactions
ENSG00000145975	chromatin interactions
ENSG00000234817	chromatin interactions
ENSG00000185689	chromatin interactions
ENSG00000112739	chromatin interactions

Extended variants
information (count: 1218 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1218 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4266528	chr6:4030708-4030709	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572116697	chr6:4030715-4030716	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541204436	chr6:4030728-4030729	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs186963109	chr6:4030772-4030773	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs192278861	chr6:4030784-4030785	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs375240206	chr6:4030833-4030834	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs1408457	chr6:4030913-4030914	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs185087624	chr6:4030926-4030927	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs723797	chr6:4030951-4030952	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs147054986	chr6:4030993-4030994	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs527915286	chr6:4031009-4031010	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs547574013	chr6:4031011-4031012	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs570857362	chr6:4031053-4031054	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533401018	chr6:4031125-4031126	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs77975055	chr6:4031139-4031140	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs723796	chr6:4031148-4031149	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs116500026	chr6:4031202-4031203	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs79200775	chr6:4031253-4031254	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs75850675	chr6:4031284-4031285	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534864479	chr6:4031352-4031353	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9392549	chr6:4031372-4031373	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs147828591	chr6:4031414-4031415	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571567924	chr6:4031448-4031449	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs9328215	chr6:4031459-4031460	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs556938536	chr6:4031469-4031470	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573585977	chr6:4031514-4031515	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542593246	chr6:4031562-4031563	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141317820	chr6:4031627-4031628	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572599588	chr6:4031700-4031701	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541227893	chr6:4031716-4031717	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564299306	chr6:4031745-4031746	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139081876	chr6:4031804-4031805	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs199974699	chr6:4031819-4031820	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190419800	chr6:4031844-4031845	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs55679507	chr6:4031861-4031862	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147543676	chr6:4031876-4031877	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148591332	chr6:4031921-4031922	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142905347	chr6:4031924-4031925	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs193218451	chr6:4031925-4031926	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200906852	chr6:4031928-4031929	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377202859	chr6:4031936-4031937	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147022134	chr6:4031955-4031956	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139067368	chr6:4031984-4031985	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs9503893	chr6:4031998-4031999	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs535082465	chr6:4032035-4032036	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138081884	chr6:4032067-4032068	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs199902453	chr6:4032069-4032070	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149525756	chr6:4032160-4032161	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs557009031	chr6:4032177-4032178	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573870996	chr6:4032247-4032248	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Uveal melanoma	20484589	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD

Chromatin state (count:1063 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4022400-4043400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:4022600-4049400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr6:4023000-4032000	Weak transcription	Fetal Muscle Trunk	muscle
4	chr6:4023000-4038600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:4023000-4063600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:4023200-4031800	Weak transcription	Placenta	Placenta
7	chr6:4023200-4034000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr6:4023200-4035600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr6:4023200-4043400	Weak transcription	Aorta	Aorta
10	chr6:4023200-4064000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:4023400-4038800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr6:4023400-4040600	Weak transcription	Fetal Brain Male	brain
13	chr6:4023400-4071600	Weak transcription	Stomach Mucosa	stomach
14	chr6:4023600-4031000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr6:4023800-4031200	Weak transcription	HUVEC	blood vessel
16	chr6:4023800-4032000	Weak transcription	Fetal Lung	lung
17	chr6:4023800-4032200	Weak transcription	Colonic Mucosa	Colon
18	chr6:4023800-4033600	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr6:4023800-4037400	Weak transcription	Fetal Brain Female	brain
20	chr6:4023800-4037600	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr6:4023800-4067000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:4024000-4031400	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr6:4024000-4031600	Weak transcription	NH-A	brain
24	chr6:4024000-4031800	Weak transcription	HMEC	breast
25	chr6:4024000-4035600	Weak transcription	NHLF	lung
26	chr6:4024000-4036400	Weak transcription	Stomach Smooth Muscle	stomach
27	chr6:4024000-4037600	Weak transcription	HSMMtube	muscle
28	chr6:4024200-4031000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr6:4024200-4031400	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr6:4024200-4037000	Weak transcription	Right Atrium	heart
31	chr6:4024200-4040200	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr6:4024400-4031800	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr6:4024400-4035800	Weak transcription	Thymus	Thymus
34	chr6:4024600-4031400	Weak transcription	Duodenum Mucosa	Duodenum
35	chr6:4024600-4031400	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr6:4024600-4031600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:4024600-4032000	Weak transcription	Fetal Muscle Leg	muscle
38	chr6:4024600-4036600	Weak transcription	Spleen	Spleen
39	chr6:4024600-4040200	Weak transcription	Esophagus	oesophagus
40	chr6:4024600-4059200	Strong transcription	Fetal Thymus	thymus
41	chr6:4025200-4031800	Weak transcription	Liver	Liver
42	chr6:4025200-4039200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr6:4025400-4037600	Weak transcription	Rectal Smooth Muscle	rectum
44	chr6:4025800-4031600	Weak transcription	Brain Germinal Matrix	brain
45	chr6:4025800-4034000	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr6:4026000-4032000	Weak transcription	Adipose Nuclei	Adipose
47	chr6:4026000-4032800	Weak transcription	Brain Anterior Caudate	brain
48	chr6:4026200-4031400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr6:4026200-4031800	Weak transcription	A549	lung
50	chr6:4027000-4032200	Weak transcription	Colon Smooth Muscle	Colon

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